OMIA 002218-9913 : Diamond-Blackfan anaemia 7 in Bos taurus
Possibly relevant human trait(s) and/or gene(s) (MIM number): 612562 (trait) Mendelian trait/disorder: unknown Considered a defect: yes Markers: Noting that mutations in the RPL11 gene (also known as ul5) result in Diamond-Blackfan anaemia 7 in humans, Zhang et al. (2020) searched for lethal RPL11 variants in cattle. Specifically, they searched for "a 2 bp deletion resulting in a frameshift and premature stop (ENSBTAG00000020905:g.129,195,922_129,195,923del; ARS‐UCD1.2; rs381576999)", a probe for which "has been included as an expert‐selected marker in the custom add‐on part of the BovineLD BeadChip". In a multi-breed panel of 370,527 cattle, the authors found "299 218 homozygous wt and 71 249 apparently heterozygous cattle but no homozygous carriers [i.e. homozygotes for the deletion]". However, the authors noted that "the BeadChip probe matches almost perfectly (49/50 nucleotides) to a processed uL5 pseudogene on BTA18 (LOC112442347; position 54 982 088–54 982 687)." The authors provided a cautionary tale in their conclusion "that there is currently no evidence for the existence of the rs381576999 indel in the functional uL5 gene . . . [but] . . . the deletion has been fixed in the pseudogene, but is not scored reliably in the BovineLD BeadChip assay. These data demonstrate how pseudogenes interfere with the scoring of high‐throughput genotyping platforms and that bead‐arrays are not suitable for assaying polymorphisms in sequences that are not single‐copy. "
|2020||Zhang, X., Wacker, C., Schütz, E., Brenig, B. :|
|Processed pseudogene confounding the identification of a putative lethal recessive deletion in the bovine 60S ribosomal protein L11 gene (uL5). Anim Genet 51:146-147, 2020. Pubmed reference: 31625165. DOI: 10.1111/age.12868.|
- Created by Frank Nicholas on 23 Oct 2019
- Changed by Frank Nicholas on 23 Oct 2019
- Changed by Frank Nicholas on 09 Apr 2020